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Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations. (2021)

First Author: Martin AR

Attributed to: Biomedical Sciences Exchange PhD studentships funded by Newton Fund

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.03.012

PubMed Identifier: 33770507

Publication URI: http://europepmc.org/abstract/MED/33770507

Type: Journal Article/Review

Volume: 108

Parent Publication: American journal of human genetics

Issue: 4

ISSN: 0002-9297